Canonical Allele Identifier: CA476282692

Gene: MRE11 MIR548L

Linked Data

• MyVariant Identifiers: chr11:g.94199714A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.94466548A>C , CM000673.2:g.94466548A>C	GRCh38
NC_000011.9:g.94199714A>C , CM000673.1:g.94199714A>C	GRCh37
NC_000011.8:g.93839362A>C	NCBI36
NG_007261.1:g.32327T>G , LRG_85:g.32327T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000323929.8:c.1098+1265T>G (MRE11) MANE Select	ENSP00000325863.4:n.1098+1265T>G
ENST00000323929.7:c.1098+1265T>G (MRE11)	ENSP00000325863.3:n.1098+1265T>G
ENST00000323977.7:c.1098+1265T>G (MRE11)	ENSP00000326094.3:n.1098+1265T>G
ENST00000393241.8:c.1098+1265T>G (MRE11)	ENSP00000376933.4:n.1098+1265T>G
ENST00000407439.7:c.1107+1265T>G (MRE11)	ENSP00000385614.3:n.1107+1265T>G
NM_005590.3:c.1098+1265T>G (MRE11)	NP_005581.2:n.1098+1265T>G
NM_005591.3:c.1098+1265T>G , LRG_85t1:c.1098+1265T>G (MRE11)	NP_005582.1:n.1098+1265T>G
NR_031630.1:n.33T>G (MIR548L)
XM_005274008.2:c.630+1265T>G (MRE11)	XP_005274065.1:n.630+1265T>G
XM_006718842.2:c.1098+1265T>G (MRE11)	XP_006718905.1:n.1098+1265T>G
XM_011542837.1:c.1098+1265T>G (MRE11)	XP_011541139.1:n.1098+1265T>G
XR_947828.1:n.1394+1265T>G (MRE11)
NM_001330347.1:c.1098+1265T>G (MRE11)	NP_001317276.1:n.1098+1265T>G
XM_005274008.3:c.630+1265T>G (MRE11)	XP_005274065.1:n.630+1265T>G
XM_006718842.3:c.1098+1265T>G (MRE11)	XP_006718905.1:n.1098+1265T>G
XM_011542837.2:c.1098+1265T>G (MRE11)	XP_011541139.1:n.1098+1265T>G
XM_017017772.1:c.1098+1265T>G (MRE11)	XP_016873261.1:n.1098+1265T>G
XR_947828.2:n.1394+1265T>G (MRE11)
NM_001330347.2:c.1098+1265T>G (MRE11)	NP_001317276.1:n.1098+1265T>G
NM_005590.4:c.1098+1265T>G (MRE11)	NP_005581.2:n.1098+1265T>G
NM_005591.4:c.1098+1265T>G (MRE11) MANE Select	NP_005582.1:n.1098+1265T>G